Approaching the Lithiation Limit of MoS 2 While Maintaining Its Layered Crystalline Structure to Improve Lithium Storage

Zhiqiang Zhu, Yuxin Tang, Wan Ru Leow, Huarong Xia, Zhisheng Lv, Jiaqi Wei, Xiang Ge, Shengkai Cao, Yanyan Zhang, Wei Zhang, Hongwei Zhang, Shibo Xi, Yonghua Du*, Xiaodong Chen

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

78 Citations (Scopus)

Abstract

MoS 2 holds great promise as high-rate electrode for lithium-ion batteries since its large interlayer can allow fast lithium diffusion in 3.0–1.0 V. However, the low theoretical capacity (167 mAh g −1 ) limits its wide application. Here, by fine tuning the lithiation depth of MoS 2 , we demonstrate that its parent layered structure can be preserved with expanded interlayers while cycling in 3.0–0.6 V. The deeper lithiation and maintained crystalline structure endows commercially micrometer-sized MoS 2 with a capacity of 232 mAh g −1 at 0.05 A g −1 and circa 92 % capacity retention after 1000 cycles at 1.0 A g −1 . Moreover, the enlarged interlayers enable MoS 2 to release a capacity of 165 mAh g −1 at 5.0 A g −1 , which is double the capacity obtained under 3.0–1.0 V at the same rate. Our strategy of controlling the lithiation depth of MoS 2 to avoid fracture ushers in new possibilities to enhance the lithium storage of layered transition-metal dichalcogenides.

Original languageEnglish
Pages (from-to)3521-3526
Number of pages6
JournalAngewandte Chemie - International Edition
Volume58
Issue number11
DOIs
Publication statusPublished - Mar 11 2019
Externally publishedYes

Bibliographical note

Publisher Copyright:
© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim

ASJC Scopus Subject Areas

  • Catalysis
  • General Chemistry

Keywords

  • commercial MoS
  • high rate
  • layered crystalline structure
  • lithiation depth
  • lithium ion batteries

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